Molecular aspects of dopaminergic neurodegeneration: gene-environment interaction in parkin dysfunction.

Authors:
Dr. Zbigniew K Binienda, DVM, PhD
Dr. Zbigniew K Binienda, DVM, PhD
FDA/NCTR
Research Scientist
Neurophysiology; Neurotoxicology
Little Rock, AR | United States

Int J Environ Res Public Health 2011 12 16;8(12):4702-13. Epub 2011 Dec 16.

Neurochemistry Laboratory, Division of Neurotoxicology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR 72029, USA.

Parkinson's disease (PD) is a common neurodegenerative movement disorder that is characterized pathologically by a progressive loss of midbrain dopaminergic neurons and by protein inclusions, designated Lewy bodies and Lewy neurites. PD is one of the most common neurodegenerative diseases, affecting almost 1% of the population over 60 years old. Although the symptoms and neuropathology of PD have been well characterized, the underlying mechanisms and causes of the disease are still not clear. Genetic mutations can provide important clues to disease mechanism, but most PD cases are sporadic rather than familial; environmental factors have long been suspected to contribute to the disease. Although more than 90% of PD cases occur sporadically and are thought to be due, in part, to oxidative stress and mitochondrial dysfunction, the study of genetic mutations has provided great insight into the molecular mechanisms of PD. Furthermore, rotenone, a widely used pesticide, and paraquat and maneb cause a syndrome in rats and mice that mimics, both behaviorally and neurologically, the symptoms of PD. In the current review, we will discuss various aspects of gene-environment interaction that lead to progressive dopaminergic neurodegenration, mainly focusing on our current finding based on stress-mediated parkin dysfunction.

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Source
http://dx.doi.org/10.3390/ijerph8124702DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3290988PMC
December 2011
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